Anatomical-functional discordance between quantitative coronary angiography and diastolic pressure ratio during

Shun Nakamura1, Taishi Yonetsu1,2, Masahiro Hoshino3

  • 1Department of Cardiovascular Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Japan.

Insights

Anatomical-functional discordance between quantitative coronary angiography (QCA) and diastolic pressure ratio (dPRWFP) is common. Predictors for this mismatch differ from those of QCA-FFR discordance, highlighting unique insights into coronary lesion assessment.

Area of Science:

  • Cardiovascular medicine
  • Interventional cardiology
  • Diagnostic imaging

Background:

  • Discrepancies between anatomical stenosis (QCA-DS) and physiological significance (dPRWFP) are common in clinical practice.
  • While QCA-FFR discordance is well-studied, predictors of QCA-dPRWFP discordance remain less understood.

Purpose of the Study:

  • To identify predictors of anatomical-functional discordance between QCA-derived diameter stenosis (QCA-DS) and dPRWFP.
  • To compare predictors of QCA-dPRWFP discordance with those of QCA-FFR discordance.

Main Methods:

  • Analysis of 647 intermediate coronary lesions (QCA-DS 30-70%) in 502 patients.
  • Determination of predictors for QCA-dPRWFP mismatch (QCA-DS >50%, dPRWFP >0.89) and reverse mismatch (QCA-DS ≤50%, dPRWFP ≤0.89).
  • FFR ≤0.80 defined as positive FFR; predictors of QCA-FFR discordance also analyzed.

Main Results:

  • QCA-dPRWFP mismatch and reverse mismatch occurred in 27.5% and 17.6% of cases.
  • Predictors for mismatch included non-LAD lesions, large minimal lumen diameter, low heart rate, and high CFR.
  • Predictors for reverse mismatch included LAD lesions, non-culprit ACS lesions, long lesion length, low LVEF, low CFR, and low IMR.

Conclusions:

  • Anatomical-functional discordance between QCA and dPRWFP is not uncommon.
  • Predictors for QCA-dPRWFP discordance differ significantly from those for QCA-FFR discordance.
  • These findings emphasize distinct factors influencing resting vs. hyperemic indices in coronary lesion assessment.
Abstract

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